Brain tumor multiple targeting drug delivery system of stability polypeptide mediated cross-barrier film
A stable and multiple technology, applied in anti-tumor drugs, drug combinations, pharmaceutical formulations, etc., can solve problems such as reducing the targeting efficiency of mediated drug delivery systems
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Embodiment 1D
[0051] Example 1 D Serum Stability of CDX and c(RGDyK)
[0052] Will D CDX or c(RGDyK) was made into a 1mg / mL solution with PBS, 0.1mL was added to 0.9mL 50% rat serum, incubated at 37°C, 100μL of the reaction solution was taken out at each time point, and acetonitrile (containing 0.1% TFA ) to precipitate the protein in the serum, let stand at 4°C for 10 minutes, centrifuge at 12000r / min for 10 minutes, take 20 μL of the supernatant for qualitative and quantitative analysis by HPLC, the results are as follows figure 1 shown.
Embodiment 2
[0053] Example 2 D Hepatic lysosomal enzyme stability of CDX and c(RGDyK)
[0054] Take fresh rat liver, add 0.3M ice sucrose solution to homogenate, centrifuge at 700×g for 10min to remove cell debris, combine the supernatant and centrifuge again, collect the supernatant and centrifuge at 10000×g for 10min, collect the precipitate and add 20mL of 0.3M sucrose solution (containing 1mM CaCl 2) and mix well, incubate at 37°C for 5min, add 20mL of 50% Percoll, centrifuge at 10000×g for 10min, collect the precipitate, resuspend with 0.3M sucrose solution, then centrifuge at 10000×g for 10min, collect the precipitate, and wash twice After three times, finally the liver lysosome homogenate obtained was resuspended with 0.3M sucrose solution, aliquoted, and stored at -80°C for future use. The protein content was determined with a BCA kit (using BSA as a standard protein to make a standard curve);
[0055] Add 100 μL of 1 mg / mL liver lysosome homogenate and 100 μL of 1 mg / mL CDX or...
Embodiment 3
[0056] Example 3 D CDX-PEG 3400 -DSPE and c(RGDyK)-PEG 3400 -Synthesis and characterization of DSPE
[0057] Will D Dissolve CDX-Cys in 0.1M PBS solution (pH7.2), take Mal-PEG 3400 -DSPE is dissolved in DMF, the two are mixed and then reacted with magnetic stirring, monitored by HPLC, and the reaction is stopped after the reaction of Mal-PEG-DSPE is complete, and the excess D CDX-Cys and DMF were dialyzed (molecular weight cut-off 3.5kDa) to remove, freeze-dried to obtain D CDX-PEG 3400 - DSPE, NMR characterizes its structure. Combine c(RGDyK)-Cys with Mal-PEG 3400 -DSPE is reacted as above to obtain c(RGDyK)-PEG 3400 -DSPE, NMR characterizes its structure (such as image 3 shown).
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